Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rumpa Mondal"'
Publikováno v:
ARKIVOC, Vol 2016, Iss 2, Pp 98-115 (2015)
Externí odkaz:
https://doaj.org/article/c072ddae33ac44bb94b5c3005adac8fe
Publikováno v:
European Journal of Organic Chemistry. 2010:3205-3210
A general process for the synthesis of substituted indenes and 1,2,3-triazoles was achieved for the first time through a multicatalysis cascade reaction of 2-ethynylbenzaldehydes, CH acids, organic hydrides, and azides in the presence of a catalytic
Publikováno v:
Org. Biomol. Chem.. 8:321-325
An efficient amino acid-/self-/base-/ruthenium-/thermal-catalyzed two-step process for the synthesis of functionalized drug-like carbocycles was achieved through combinations of cascade TCRA/C-allylation/enyne-RCM/Diels-Alder reactions as key steps s
Publikováno v:
Tetrahedron Letters. 47:7689-7693
The direct addition of a variety of alcohols to in situ activated olefins was observed in the presence of mild bifunctional amine/acid catalysts. Unlike existing methods, the reactions proceed at room temperature and in the absence of transition meta
Publikováno v:
Organicbiomolecular chemistry. 10(26)
A high-yielding asymmetric synthesis of functionalized (2-ethynylphenyl)alcohols 5/6 with good diastereo- and enantioselectivities was achieved by Barbas-List aldol (BLA) reaction of 2-alkynylbenzaldehydes 1 with various ketones 2 in the presence of
Publikováno v:
ChemInform. 41
The iminium activation of aldehydes, the self-activation of olefins, and the simultaneous activation of metal ion alkynes are combined in a cascade sequence, constituting a new carbocyclization method to furnish indenes through a Conia-ene reaction,
Publikováno v:
ChemInform. 41
An efficient amino acid-/self-/base-/ruthenium-/thermal-catalyzed two-step process for the synthesis of functionalized drug-like carbocycles was achieved through combinations of cascade TCRA/C-allylation/enyne-RCM/Diels–Alder reactions as key steps
Publikováno v:
ChemInform. 39
The three-component Friedel–Crafts alkylation/Huisgen cycloaddition (FCA/HC) reactions of 2-naphthols, substituted isatins and azides under dimethylamino-ethanol/Cu I -catalysis furnished highly functionalized 1,4-disubstituted [1,2,3]-triazoles.